Litcius/Paper detail

Oxidative Halogenation of Arenes, Olefins and Alkynes Mediated by Iodine(III) Reagents

Luis A. Segura‐Quezada, Karina R. Torres‐Carbajal, Yuvraj Satkar, Kevin Arturo Juárez Ornelas, Narendra Mali, Dipak Patil, Rocío Gámez‐Montaño, Juan R. Zapata-Morales, Selene Lagunas‐Rivera, Rafael Ortíz‐Alvarado, César R. Solorio‐Alvarado

2020Mini-Reviews in Organic Chemistry21 citationsDOI

Abstract

Iodine(III)-based reagents have been broadly used in oxidative reactions for structural functionalization with several functional groups. Among the more relevant and useful synthetic transformations using these hypervalent λ 3 -reagents, the fluorination, chlorination, bromination, as well as the iodination protocols, can be found. Herein, we present some of the most representative oxidative halogenation procedures of arenes, olefins and alkynes dating from the oldest to the more recent advances in the area, highlighting the discovery and application of new iodine(III)-based halogenating species.

Topics & Concepts

Hypervalent moleculeHalogenationIodineReagentChemistryOxidative phosphorylationOrganic chemistrySurface modificationCombinatorial chemistryIodine compoundsBiochemistryPhysical chemistryVanadium and Halogenation Chemistry